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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1045403Erstellt: 26. Oktober 2026

Isopropanol → 2-(benzyloxymethyl)-3,4-dihydro-2H-pyran

https://huagongshe.com/reaction/1045403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
EduktSodium HydroxideHCID 14798—
Edukt((2-(Allyloxy)pent-4-enyloxy)methyl)benzeneHCID 12996273—
KatalysatorGrubbs CatalystHCID 6392641—
KatalysatorBenzylidenebis(tricyclohexylphosphine)dichlororutheniumHCID 11967259—
LösungsmittelTolueneHCID 1140—
Produkt2-(benzyloxymethyl)-3,4-dihydro-2H-pyranHCID 4095658—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium, bis(tricyclohexylphosphine) benzylidine ruthenium(IV) chloride—Grubbs 1 generation catalyst (0.5 g, 0.54 mmol) was added in one portion to a stirred solution of ((2-(allyloxy)pent-4-enyloxy)methyl)benzene (12) (4 g, 17.2 mmol) in toluene (200 mL). The resulting mixture was heated at 50° C. under N2 for 2 hours before isopropanol (18 mL) and NaOH (0.17 g) were added. The mixture was then heated at 120° C. overnight. The solvent was evaporated and the residue was purified over silica gel using Et2O and hexane to give 2-(benzyloxymethyl)-3,4-dihydro-2H-pyran (13).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08569283B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-4c0b433d4a6b4a059af057edae0e945c
Quellennotizuspto-grants-2013_10